NAGK N-acetylglucosamine kinase
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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68 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
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Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | GNK |
SYNONYM | HSA242910 |
MIM | 606828 OMIM |
HGNC | HGNC:17174 HGNC |
Ensembl | ENSG00000124357 Ensembl |
AllianceGenome | HGNC:17174 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000443872.6 | hg38 | chr2 | 71,068,592 | 71,078,585 | 9,994 |
ENST00000443938.6 | hg38 | chr2 | 71,068,619 | 71,078,641 | 10,023 |
ENST00000244204.11 | hg38 | chr2 | 71,068,648 | 71,079,808 | 11,161 |
ENST00000418807.7 | hg38 | chr2 | 71,068,588 | 71,079,805 | 11,218 |
ENST00000455662.6 | hg38 | chr2 | 71,068,301 | 71,078,868 | 10,568 |
ENST00000613852.4 | hg38 | chr2 | 71,068,278 | 71,078,868 | 10,591 |
ENST00000613852.4 | hg19 | chr2 | 71,295,408 | 71,305,998 | 10,591 |
ENST00000455662.6 | hg19 | chr2 | 71,295,431 | 71,305,998 | 10,568 |
ENST00000418807.7 | hg19 | chr2 | 71,295,718 | 71,306,935 | 11,218 |
ENST00000443872.6 | hg19 | chr2 | 71,295,722 | 71,305,715 | 9,994 |
ENST00000443938.6 | hg19 | chr2 | 71,295,749 | 71,305,771 | 10,023 |
ENST00000244204.11 | hg19 | chr2 | 71,295,778 | 71,306,938 | 11,161 |
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